List of variants in gene BARD1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.33G>T (p.Gln11His)	rs143914387	0.00176
NM_000465.4(BARD1):c.1347A>G (p.Gln449=)	rs373257776	0.00021
NM_000465.4(BARD1):c.57G>A (p.Glu19=)	rs730881406	0.00019
NM_000465.4(BARD1):c.1409A>G (p.Asn470Ser)	rs587781976	0.00008
NM_000465.4(BARD1):c.1586G>A (p.Arg529Gln)	rs753479021	0.00006
NM_000465.4(BARD1):c.1194A>G (p.Thr398=)	rs781482219	0.00002
NM_000465.4(BARD1):c.117C>T (p.Ala39=)	rs786202271
NM_000465.4(BARD1):c.1479A>G (p.Gln493=)	rs375029767
NM_000465.4(BARD1):c.1914A>G (p.Ala638=)	rs876658489
NM_000465.4(BARD1):c.2163A>G (p.Ala721=)	rs786202805

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